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Multifaceted Mechanisms of Action of Metformin Which Have Been Unraveled One after Another in the Long History

While there are various kinds of drugs for type 2 diabetes mellitus at present, in this review article, we focus on metformin which is an insulin sensitizer and is often used as a first-choice drug worldwide. Metformin mainly activates adenosine monophosphate-activated protein kinase (AMPK) in the l...

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Autores principales: Kaneto, Hideaki, Kimura, Tomohiko, Obata, Atsushi, Shimoda, Masashi, Kaku, Kohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962041/
https://www.ncbi.nlm.nih.gov/pubmed/33807522
http://dx.doi.org/10.3390/ijms22052596
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author Kaneto, Hideaki
Kimura, Tomohiko
Obata, Atsushi
Shimoda, Masashi
Kaku, Kohei
author_facet Kaneto, Hideaki
Kimura, Tomohiko
Obata, Atsushi
Shimoda, Masashi
Kaku, Kohei
author_sort Kaneto, Hideaki
collection PubMed
description While there are various kinds of drugs for type 2 diabetes mellitus at present, in this review article, we focus on metformin which is an insulin sensitizer and is often used as a first-choice drug worldwide. Metformin mainly activates adenosine monophosphate-activated protein kinase (AMPK) in the liver which leads to suppression of fatty acid synthesis and gluconeogenesis. Metformin activates AMPK in skeletal muscle as well, which increases translocation of glucose transporter 4 to the cell membrane and thereby increases glucose uptake. Further, metformin suppresses glucagon signaling in the liver by suppressing adenylate cyclase which leads to suppression of gluconeogenesis. In addition, metformin reduces autophagy failure observed in pancreatic β-cells under diabetic conditions. Furthermore, it is known that metformin alters the gut microbiome and facilitates the transport of glucose from the circulation into excrement. It is also known that metformin reduces food intake and lowers body weight by increasing circulating levels of the peptide hormone growth/differentiation factor 15 (GDF15). Furthermore, much attention has been drawn to the fact that the frequency of various cancers is lower in subjects taking metformin. Metformin suppresses the mechanistic target of rapamycin (mTOR) by activating AMPK in pre-neoplastic cells, which leads to suppression of cell growth and an increase in apoptosis in pre-neoplastic cells. It has been shown recently that metformin consumption potentially influences the mortality in patients with type 2 diabetes mellitus and coronavirus infectious disease (COVID-19). Taken together, metformin is an old drug, but multifaceted mechanisms of action of metformin have been unraveled one after another in its long history.
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spelling pubmed-79620412021-03-17 Multifaceted Mechanisms of Action of Metformin Which Have Been Unraveled One after Another in the Long History Kaneto, Hideaki Kimura, Tomohiko Obata, Atsushi Shimoda, Masashi Kaku, Kohei Int J Mol Sci Review While there are various kinds of drugs for type 2 diabetes mellitus at present, in this review article, we focus on metformin which is an insulin sensitizer and is often used as a first-choice drug worldwide. Metformin mainly activates adenosine monophosphate-activated protein kinase (AMPK) in the liver which leads to suppression of fatty acid synthesis and gluconeogenesis. Metformin activates AMPK in skeletal muscle as well, which increases translocation of glucose transporter 4 to the cell membrane and thereby increases glucose uptake. Further, metformin suppresses glucagon signaling in the liver by suppressing adenylate cyclase which leads to suppression of gluconeogenesis. In addition, metformin reduces autophagy failure observed in pancreatic β-cells under diabetic conditions. Furthermore, it is known that metformin alters the gut microbiome and facilitates the transport of glucose from the circulation into excrement. It is also known that metformin reduces food intake and lowers body weight by increasing circulating levels of the peptide hormone growth/differentiation factor 15 (GDF15). Furthermore, much attention has been drawn to the fact that the frequency of various cancers is lower in subjects taking metformin. Metformin suppresses the mechanistic target of rapamycin (mTOR) by activating AMPK in pre-neoplastic cells, which leads to suppression of cell growth and an increase in apoptosis in pre-neoplastic cells. It has been shown recently that metformin consumption potentially influences the mortality in patients with type 2 diabetes mellitus and coronavirus infectious disease (COVID-19). Taken together, metformin is an old drug, but multifaceted mechanisms of action of metformin have been unraveled one after another in its long history. MDPI 2021-03-05 /pmc/articles/PMC7962041/ /pubmed/33807522 http://dx.doi.org/10.3390/ijms22052596 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kaneto, Hideaki
Kimura, Tomohiko
Obata, Atsushi
Shimoda, Masashi
Kaku, Kohei
Multifaceted Mechanisms of Action of Metformin Which Have Been Unraveled One after Another in the Long History
title Multifaceted Mechanisms of Action of Metformin Which Have Been Unraveled One after Another in the Long History
title_full Multifaceted Mechanisms of Action of Metformin Which Have Been Unraveled One after Another in the Long History
title_fullStr Multifaceted Mechanisms of Action of Metformin Which Have Been Unraveled One after Another in the Long History
title_full_unstemmed Multifaceted Mechanisms of Action of Metformin Which Have Been Unraveled One after Another in the Long History
title_short Multifaceted Mechanisms of Action of Metformin Which Have Been Unraveled One after Another in the Long History
title_sort multifaceted mechanisms of action of metformin which have been unraveled one after another in the long history
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962041/
https://www.ncbi.nlm.nih.gov/pubmed/33807522
http://dx.doi.org/10.3390/ijms22052596
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